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STERILUCENT SELF-SEAL STERILIZATION POUCH

K141412 Class II Traditional
Decision Date
2014-12-03
Sponsor / Applicant
Gs Medical Packaging, Inc.

Technical Specification

510(k) Submission ID K141412
Product Code FRG
Medical Specialty / Panel General Hospital
Regulation Citation 21 CFR 880.6850
Decision Date 2014-12-03
Clearance Pathway Traditional

Official Documentation

FDA CDRH Summary / statement of record

View FDA Summary PDF

Clearance Summary

STERILUCENT SELF-SEAL STERILIZATION POUCH received FDA 510(k) clearance under submission number K141412, sponsored by Gs Medical Packaging, Inc.. The device was reviewed via the Traditional premarket notification pathway and assigned to the General Hospital review panel. The statutory decision date of record is 2014-12-03.

Classification & Regulation

This clearance is catalogued under FDA product code FRG and 21 CFR 880.6850, within the General Hospital review panel as a Class II device.